tert-butyl 1-iminothiomorpholine-4-carboxylate 1-oxide

95%

Reagent Code: #242805
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CAS Number 1609964-38-6

science Other reagents with same CAS 1609964-38-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.3173 g/mol
Formula C₉H₁₈N₂O₃S
badge Registry Numbers
MDL Number MFCD30183341
inventory_2 Storage & Handling
Storage 2-8°C, preserved from light, dry sealed

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting enzyme inhibition. Its unique thiomorpholine ring structure with a tert-butyl protecting group enables selective reactivity in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and antimicrobial agents due to its ability to mimic peptide bonds and interact with active sites of enzymes. Also utilized in agrochemical research for designing novel pesticides with improved stability and target specificity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,400.00
inventory 250mg
10-20 days ฿20,640.00
inventory 1g
10-20 days ฿62,110.00

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tert-butyl 1-iminothiomorpholine-4-carboxylate 1-oxide
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting enzyme inhibition. Its unique thiomorpholine ring structure with a tert-butyl protecting group enables selective reactivity in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and antimicrobial agents due to its ability to mimic peptide bonds and interact with active sites of enzymes. Also utilized in agrochemical research for

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting enzyme inhibition. Its unique thiomorpholine ring structure with a tert-butyl protecting group enables selective reactivity in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and antimicrobial agents due to its ability to mimic peptide bonds and interact with active sites of enzymes. Also utilized in agrochemical research for designing novel pesticides with improved stability and target specificity.

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